Regulatory Affairs Biosimilars Per Diem Consultant
Pharmavise Corporation · Remote · remote · Posted 36d ago
Undisclosed8–13 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Summary
This is a remote position.
We are actively seeking skilled and knowledgeable professionals to join our team as Regulatory Affairs Biosimilars Per Diem Consultants. Below, youll find a comprehensive job description detailing the responsibilities, qualifications, and expectations for this role:
Responsibilities
- Provide expert regulatory affairs guidance and support for biosimilars development projects.
- Review and analyze regulatory requirements and guidelines related to biosimilars in various regions.
- Assist in the preparation, submission, and maintenance of regulatory submissions for biosimilars, including INDs, BLAs, and variations.
- Collaborate with cross-functional teams to ensure alignment on regulatory strategy and objectives.
- Stay updated on regulatory developments and trends impacting biosimilars globally.
- Participate in meetings with regulatory authorities as needed.
- Provide regulatory support and expertise during regulatory agency inspections and audits.
Qualifications
- Bachelors degree in a scientific or related field; advanced degree preferred.
- Minimum of 8 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with specific expertise in biosimilars preferred.
- Strong understanding of regulatory requirements and guidelines governing biosimilars development and approval processes.
- Experience with regulatory submissions for biosimilars, including INDs, BLAs, and variations.
- Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders.
- Proven ability to work independently and manage multiple projects simultaneously.
- Regulatory affairs certification (RAC) preferred but not required.
Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
Regulatory Affairsregulatory submissionsauditsRACBiotechnologySubject MatterRegulatory ComplianceManufacturingmaintenancecompliancePharmaceuticalCommunication And Interpersonal Skills